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NCT04551586 · ClinicalTrials.gov registry record · Phase 1

A Study to Assess ACH-0145228 When Administered as Immediate Release Tablet Versus Powder-In-Capsule in Healthy Adult Participants

A Phase 1 study of Healthy, sponsored by Alexion Pharmaceuticals.

Completed
Registry status
Phase 1
Development phase
28
Enrollment target
1
Study location

NCT04551586: Completed Phase 1 study of Healthy, sponsored by Alexion Pharmaceuticals.

NCT04551586 is a Phase 1 study of Healthy that has completed, run by Alexion Pharmaceuticals. The registered enrollment target is 28 participants, below the 647-participant average among 1,090 other Healthy trials with a reported enrollment target (96% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04551586, a Phase 1 study of Healthy, has completed, sponsored by Alexion Pharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
28 participants
Enrollment target
1
Study location

Study Summary

This will be an open-label, 3-sequence, 3-period crossover study in healthy adult participants to assess the relative bioavailability of ACH-0145228 when administered as an immediate release tablet versus powder-in-capsule.

Conditions Studied

Interventions

  • DRUG ACH-0145228: Immediate Release
  • DRUG ACH-0145228: Powder-in-capsule

Study Locations (1)

Nebraska

  • Clinical Trial Site - Lincoln

Trial Details

FieldValue
Enrollment Target 28 participants
Start Date 2020-06-26
Est. Completion 2020-10-19
Phase Phase 1

Sponsor

Alexion Pharmaceuticals

162 total trials

What the Registry Record Tells You About NCT04551586

The ClinicalTrials.gov registry entry for NCT04551586 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 28 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 647-participant average among 1,090 other Healthy trials with a reported enrollment target (96% lower). The listed sponsor is Alexion Pharmaceuticals, which has 162 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Healthy appearing as the primary indexed condition, and to 2 interventions - of which ACH-0145228: Immediate Release is the first listed.

NCT04551586 reports 1 study location spanning 1 distinct geographic area - top geographies include Nebraska.

Frequently Asked Questions

What is clinical trial NCT04551586 about?

NCT04551586 is a clinical study titled "A Study to Assess ACH-0145228 When Administered as Immediate Release Tablet Versus Powder-In-Capsule in Healthy Adult Participants". This will be an open-label, 3-sequence, 3-period crossover study in healthy adult participants to assess the relative bioavailability of ACH-0145228 when administered as an immediate release tablet versus powder-in-capsule.

What is the current status of trial NCT04551586?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 28 participants. The study started on 2020-06-26. Estimated completion is 2020-10-19.

What conditions does trial NCT04551586 study?

This clinical trial studies the following conditions: Healthy.

What interventions are being tested in trial NCT04551586?

The interventions under investigation include: ACH-0145228: Immediate Release (DRUG), ACH-0145228: Powder-in-capsule (DRUG).

Who is sponsoring clinical trial NCT04551586?

This trial is sponsored by Alexion Pharmaceuticals, which has 162 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04551586 being conducted?

This trial has 1 study location across Nebraska. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, the data changelog, or report a data error.